Tetraploid Partial Hydatidiform Moles: Molecular Genotyping and Determination of Parental Contributions

Jennifer Bynum, Denise Batista, Rena Xian, Deyin Xing, James R. Eshleman, Brigitte M. Ronnett, Gang Zheng

Research output: Contribution to journalArticle

Abstract

DNA genotyping studies have established that most partial hydatidiform moles (PHMs) are diandric dispermic triploid conceptions. Rare triandric tetraploid PHMs have been described, but genotyping cannot determine the manner in which three paternal chromosome complements are derived (one sperm with triplication, two sperm with one duplication, three different sperm, or one diploid and one haploid sperm). In a large prospective analysis of potentially molar products of conception, five tetraploid PHMs were encountered among 235 PHMs. Single-nucleotide polymorphism (SNP) arrays were used to define different paternal chromosomal contributions. Short tandem repeat analysis of the five tetraploid PHMs established that these contained three paternal and one maternal chromosome complements. In each case, the corresponding SNP array found five tracts with segmented absence of the central tract across approximately 25% of the genome. Meiotic crossovers could be observed directly in the chromosomes via the total number of starts and stops of regions of loss of heterozygosity. The findings are consistent with each conceptus having three different paternal contributions and one maternal contribution. These findings suggest that tetraploid PHMs arise when three different sperm fertilize a single, normal ovum. SNP array is useful to determine the parental contributions in triploid/tetraploid conceptuses. It also allows for direct visualization of meiotic crossover frequency and sites in these conceptions, providing insight into their biology.

Original languageEnglish (US)
Pages (from-to)90-100
Number of pages11
JournalJournal of Molecular Diagnostics
Volume22
Issue number1
DOIs
StatePublished - Jan 2020

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ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Molecular Medicine

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